Method for preparing probiotic microcapsule by utilizing spray drying
A technology of probiotics and microcapsules, applied in the field of microorganisms, can solve the problem of high bacterial mortality, achieve the effect of ensuring the number of viable bacteria and increasing tolerance
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[0024] Example one:
[0025] A method for preparing probiotic microcapsules by spray drying includes the following steps:
[0026] 1. Preparation of culture medium: The culture medium is made up of the following parts by weight: 5 parts of yeast powder, 10 parts of peptone, 20 parts of glucose, 5 parts of sodium acetate trihydrate, 0.5 parts of magnesium sulfate heptahydrate, and 2 parts of potassium hydrogen phosphate. Parts, 2 parts of diammonium citrate, 10 parts of meat extract, 0.05 parts of manganese sulfate tetrahydrate, Tween-801 parts, 1000 parts of purified water; mix yeast powder, peptone, glucose, sodium acetate trihydrate, magnesium sulfate heptahydrate , Dipotassium hydrogen phosphate, diammonium citrate, meat extract 10, manganese sulfate tetrahydrate, Tween-80 in accordance with the ratio, pour into purified water and heat to dissolve, dissolve, disassemble, and place in a sterilization pot at 121℃ Sterilize for 20 minutes under the conditions, and set aside;
[002...
Example Embodiment
[0038] Embodiment two:
[0039] The basic steps of this embodiment are the same as the first embodiment, the difference is: in step 3, place the culture in a 37°C incubator. After 12 hours of incubation, put the petri dish into a 70°C constant temperature water bath and bath for 5 minutes.
Example Embodiment
[0040] Example three:
[0041] The basic steps of this embodiment are the same as those of the first embodiment. The difference is: in step 3, the culture is placed in a 37°C incubator. After 13 hours of cultivation, the petri dish is placed in a 80°C constant temperature water bath and the water bath is bathed for 6 minutes.
[0042] The comparison table of the embodiment of the present invention and the existing preparation method under the same experimental conditions:
[0043]
[0044] It can be seen from the above table that, compared with the existing preparation method, the product of the present invention can effectively increase the number of viable bacterial powder.
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